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苯丙胺、哌醋甲酯和阿扑吗啡对脑局部5-羟色胺及5-羟吲哚乙酸的影响。

Effects of amphetamine, methylphenidate, and apomorphine on regional brain serotonin and 5-hydroxyindole acetic acid.

作者信息

Kuczenski R, Segal D S, Leith N J, Applegate C D

机构信息

Department of Psychiatry, University of California, San Diego, La Jolla 92093.

出版信息

Psychopharmacology (Berl). 1987;93(3):329-35. doi: 10.1007/BF00187252.

Abstract

Electrophysiological and cytofluorometric data suggest that doses of amphetamine which enhance locomotor activity and promote focused stereotypies produce pronounced effects on serotonin pathways in the CNS. However, the biochemical evidence regarding changes in serotonergic function produced by moderate doses of this drug is inconsistent. Therefore, the present study was designed to further examine the effects of amphetamine (1-5 mg/kg) on regional brain serotonin and its metabolite and to compare these effects to behaviorally comparable doses of methylphenidate and apomorphine. At doses which produce a multiphasic behavioral response pattern, including a stereotypy phase consisting primarily of repetitive head movements and occasional oral stereotypies, amphetamine (3 mg/kg) and methylphenidate (30 mg/kg) increased levels of 5HIAA in striatum and frontal cortex, two brain regions which receive serotonergic projections from the dorsal raphe nucleus. In contrast, these drugs decreased or had no effect on 5HIAA levels in hippocampus, a brain region which receives its serotonergic innervation from the median raphe nucleus. A moderate dose of apomorphine (0.5 mg/kg) produced a comparable pattern of neurochemical effects. These data are consistent with electrophysiological and cytofluorometric data suggesting enhanced dorsal raphe serotonergic function following amphetamine-like stimulants. Pretreatment of animals with alpha-methyltyrosine at a dose sufficient to prevent the locomotor stimulation and stereotypy promoted by amphetamine, or by haloperidol, failed to prevent the amphetamine-induced increase in 5HIAA, indicating that these serotonergic effects are not secondary to the amphetamine facilitation of dopaminergic transmission.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

电生理和细胞荧光测定数据表明,能增强运动活性并促进刻板行为的苯丙胺剂量,会对中枢神经系统中的血清素通路产生显著影响。然而,关于该药物中等剂量所产生的血清素能功能变化的生化证据并不一致。因此,本研究旨在进一步检测苯丙胺(1 - 5毫克/千克)对脑区血清素及其代谢物的影响,并将这些影响与行为学上等效剂量的哌甲酯和阿扑吗啡进行比较。在产生多相行为反应模式(包括主要由重复性头部运动和偶尔的口部刻板行为组成的刻板行为阶段)的剂量下,苯丙胺(3毫克/千克)和哌甲酯(30毫克/千克)提高了纹状体和额叶皮质中5 - 羟吲哚乙酸(5HIAA)的水平,这两个脑区接受来自中缝背核的血清素能投射。相比之下,这些药物降低了海马体中5HIAA的水平或对其没有影响,海马体是一个从中缝正中核接受血清素能神经支配的脑区。中等剂量的阿扑吗啡(0.5毫克/千克)产生了类似的神经化学效应模式。这些数据与电生理和细胞荧光测定数据一致,表明在苯丙胺类兴奋剂作用后中缝背核血清素能功能增强。用足以防止苯丙胺促进的运动刺激和刻板行为的剂量的α - 甲基酪氨酸或氟哌啶醇对动物进行预处理,未能阻止苯丙胺诱导的5HIAA增加,这表明这些血清素能效应并非继发于苯丙胺对多巴胺能传递的促进作用。(摘要截选至250字)

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